"Revvity Omics, Revvity"[submitter] AND "VCL"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 202151	NM_014000.3(VCL):c.224C>T (p.Pro75Leu)	VCL (P75L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GUncertain significance
Select item 1437525	NM_014000.3(VCL):c.875G>T (p.Gly292Val)	VCL (G292V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 582278	NM_014000.3(VCL):c.1648C>G (p.Gln550Glu)	VCL (Q550E)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W +2 more	GUncertain significance
Select item 837767	NM_014000.3(VCL):c.2030C>T (p.Ser677Leu)	VCL (S677L)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 202149	NM_014000.3(VCL):c.2467C>T (p.Arg823Trp)	VCL (R823W)	Single nucleotide variant (missense variant)	Cardiomyopathy +3 more	GUncertain significance
Select item 300797	NM_014000.3(VCL):c.2807C>T (p.Ala936Val)	VCL (A936V)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype +3 more	GUncertain significance
Select item 45602	NM_014000.3(VCL):c.2862_2864del (p.Leu955del)	VCL (L955del)	Deletion (inframe_deletion +1 more)	Dilated cardiomyopathy 1W +5 more	GConflicting classifications of pathogenicity

ClinVar